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<front>
<journal-meta>
<journal-id journal-id-type="issn">1043-3155</journal-id>
<journal-id journal-id-type="nlm-ta">Pediatr Neurol Briefs</journal-id>
<journal-id journal-id-type="pmc">pedneurbriefs</journal-id>
<journal-id journal-id-type="iso-abbrev">Pediatr Neurol Briefs</journal-id>
<journal-title-group>
<journal-title>Pediatric Neurology Briefs</journal-title>
<abbrev-journal-title>Pediatr Neurol Briefs</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2166-6482</issn>
<issn pub-type="ppub">1043-3155</issn>
<issn-l>2166-3155</issn-l>
<publisher>
<publisher-name>Pediatric Neurology Briefs Publishers</publisher-name>
<publisher-loc>Chicago, IL, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">PNB-8-51-b</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-8-7-5</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Seizure Disorders</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Neurology</subject>
<subject>Pediatrics</subject>
<subject>Nervous System Diseases</subject>
<subject>Child Development</subject>
<subject>Brain Diseases</subject>
<subject>Neurosurgery</subject>
<subject>Child</subject>
<subject>Infant</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Cortical Hypometabolism in West&#x2019;s Syndrome</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0173-7931</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>J. Gordon</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Children&#x0027;s Memorial Hospital, Chicago, IL</aff>
<aff id="AF0002">
<label>2</label>Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. J. Gordon Millichap, E-mail: <email xlink:href="jgmillichap@northwestern.edu">jgmillichap@northwestern.edu</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>07</month>
<year>1994</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>06</month>
<year>2016</year>
</pub-date>
<volume>8</volume>
<issue>7</issue>
<fpage>51</fpage>
<lpage>51</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1994 The Author(s)</copyright-statement>
<copyright-year>1994</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under the <uri xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</uri>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<related-article id="R1" related-article-type="commentary-article" ext-link-type="doi" xlink:href="10.1016/S0140-6736(94)93065-1" vol="343" page="1620">
<article-title>Evolutional changes of cortical hypometabolism in West&#x2019;s syndrome</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The association between changes on serial PET studies and the clinical course of 12 patients with newly diagnosed West&#x2019;s syndrome is reported from the Departments of Pediatrics and Radiology, Nagoya University School of Medicine, Nagoya, Japan.</p>
</abstract>
<kwd-group>
<kwd>West&#x2019;s Syndrome</kwd>
<kwd>Focal Cortical Hypometabolism</kwd>
<kwd>Psychomotor</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The association between changes on serial PET studies and the clinical course of 12 patients with newly diagnosed West&#x2019;s syndrome is reported from the Departments of Pediatrics and Radiology, Nagoya University School of Medicine, Nagoya, Japan. PET with FDG revealed diffuse or focal cortical hypometabolism in 11 patients, whereas MRI showed abnormalities in only 5. In 7 patients with normal findings on a second PET, spasms ceased after treatment, whereas in 5 with persistent abnormalities on PET, spasms persisted or recurred or partial seizures developed. Patients with normal MRI and normal second PET studies had normal psychomotor development. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p>COMMENT. PET has been found of value in the preoperative evaluation of patients with West&#x2019;s syndrome [<xref ref-type="bibr" rid="CIT0002">2</xref>]. It may also be used in the assessment of prognosis. See also <underline>Ped Neur Briefs</underline> March 1992 and <underline>Progress in Pediatric Neurology II</underline>, Chicago, PNB Publ, 1994, for further reference to PET and infantile spasms.</p>
</disp-quote>
</body>
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